X-Message-Number: 14609
From: "Igor Artyuhov" <>
Subject: Perftoran: possible use in cryonics?
Date: Tue, 3 Oct 2000 16:06:14 +0400

Perftoran is a blood substitute that was developed in Russia as long as
about 20 years ago, but only recently approved for medical usage. In fact it
was widely used by military medics during the war in Afghanistan to treat
massive blood losses, burnings et al. At that time it has saved many
soldiers' lives, but due to some cases of side effects it wasn't approved
for general application.

As recent studies revealed, except for rare cases of individual intolerance,
majority of side effects occurred due to either improper quality of product
or improper conditions of storage. About a year ago Perftoran was approved
for application in Russia.

It happened that Perftoran, being developed as oxygen carrying blood
substitute, has many more interesting features. Among them are:
- ability to diminish blood viscosity, thus improving blood circulation in
thin vessels,
- antioxidative properties,
- ability to stabilize cell membranes and
- sorbtion properties.
Intravenal injections of Perftoran distinctly improved state of patients
with brain or heart ischemia.

It seems to me worth studying the possibilities to use Perftoran either as a
component of perfusion liquid for cryopreservation, or for pre-mortem
injections to diminish impact of ischemia, or both.

Igor Artyuhov,


------------------------------------------------

Ministry of Health of Russian Federation

Approved by: Pharmacologic State Committee
24" June 1999

Instruction
for medical application of Perftoran preparation

Perftoranum

Registration number 96/50/10

Description

Perftoran is 10 volume % emulsion on the base of perfluoroorganic compounds
(PFOC), stabilized by 4% surface-active substance (SAS) - Proxanol 268 at
average size of emulsion particles 0,03-0,15mkm. It has the following
electrolitic composition: sodium chloride - 0,6; potassium chloride - 0,39;
magnesium chloride - 0,19; sodium hydrocarbonate - 0,65; sodium hydro
phosphate - 0,2; glucose - 2,0; Osmomolarity - 280-310 mOsm/l, pH 7.2 - 7.8.
Oxygen solubility 6-7 vol.% (at pO2=760 mm of mercury column). This emulsion
has white colour with slightly blue tint, without smell.

Pharmacological properties

Perftoran - blood substitute preparation with gas-transport function. It is
used as an antishock and anti-ischemic agent. The preparation is possessed
of rheological, hemodynamic, diuretic, membranestabilizing, cardioprotective
and sorbtion properties.

Pharmacokinetics

Half-life period of Perftoran from blood bed is about 24 hours.
Surface-active substances are eliminated from the body via kidney during the
first day. Perfluorocarbons are chemically inactive and are not metabolized
in the body. Perfluorocarbons are eliminated from body via lungs in expired
air during 18-24 month.

Indications for application

Perftoran is used as a blood substitute preparation with gas transporting
function in case of shock, blood losses, multiple trauma, burning of large
surface of skin, conditions of apparent death as well as in transplantology.

Contraindications

Perftoran is contraindicated in patients with hemophilia; at pregnancy it
can be used according to vital readings.
Perftoran should not be mixed (in one syringe, infusion system or artificial
circulation apparatus) with dextrans, polyglucin, reopolyglucin and
oxyethylstarch. Use these solutions after the administration of Perftoran or
through other peripheral venous access.

Method of use and doses

Before Perftoran infusion physician should make sight examine of the
preparation. The preparation is applicable if there are no any breaks on the
bottle, vacuum packing and the label is preserved. The results of sight
examination of the bottles and label's data (name of the preparation,
manufacturer, series number) should be registered in clinical records.

At Perftoran application the biological test is obligatory: after the slow
administration of first 5 and following 30 drops it is recommended to make a
break for 3 minutes.

If there is no any reaction the infusion of the preparation is continued.
The results of biotest are registered in clinical records. Perftoran is
administered as a drip or continuous infusion in the dose of 5 ml/kg to 30
ml/kg (adults). Single and total doses of the preparation depend on
emergency of initial patient' s state and age. To achieve maximum effect the
patient should receive adequate oxygenation (40-60%) during 24 hours after
or during the infusion. For anti-ischemic protection of transplantants
Perftoran is used in artificial circulation apparatus as a perfusate at a
dose of 10-40 ml/kg.

Side effects

The injection of Perftoran can cause allergic reactions (urticaria, skin
itch, redness of skin), tachicardia, decrease in blood pressure,
hypertermia, headache, chest pain and lumbal pain, difficulty in breathing,
anaphylactoid reaction. When adverse reactions occur, the infusion of
Perftoran should be stopped and desensibilization, heart-tone,
glucocorticoids, vasopressors and other medicaments, which are used in
therapy of anaphylactic shock, should be administered without taking out a
needle from a vein.

Presentation

Glass vials containing 50, 100, 200 and 400 ml.

Storage

Perftoran should be stored frozen at the temperature -4 C to -18 C.
Perftoran can be stored after thawing at the temperature +4 C no longer than
2 weeks in refrigerator. The preparation is recommended to thaw at room
temperature. After thawing the preparation should be thoroughly shook to
receive the homogeneous composition and before the infusion it should be
warmed up to +21 C - +23 C.

Perftoran may be thawed and refrozen 5 times.

The preparation is not suitable for application in case of:
 	Stratification of emulsion (transparent oily drops on the vial bottom even
after shaking);
 	Appearance of white sediment on the vial bottom.

It is prohibited:
 	to thaw the preparation at temperatures above +30 C.
 	to store the preparation at temperatures below -18 C.

Shelf life

The shelf life is 3 years at the temperature -4 C to -18 C and 2 weeks at
the temperature no higher than +4 C.

The preparation is delivered under the doctor's prescriptions.

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